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Silica nanoparticles as drug delivery system for immunomodulator GMDP /

The development of nanosystems for topical drug delivery to target cells is a promising tool to improve the drug therapeutic index. Transport systems can be designed to control the dispatch of the loaded drug to target areas, increasing its local concentration and bioavailability, while prolonging i...

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Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Parfenyuk, E. V.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York, N.Y. : [New York, N.Y.] (222 East 46th Street, New York, NY 10017) : ASME ; Momentum Press, 2012.
Colección:Biomedical & nanomedical technologies.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Silica nanoparticles as drug delivery system for immunomodulator GMDP /  |c E.V. Parfenyuk [and others]. 
260 |a New York, N.Y. :  |b ASME ;  |a [New York, N.Y.] (222 East 46th Street, New York, NY 10017) :  |b Momentum Press,  |c 2012. 
300 |a 1 online resource (x, 69 pages) :  |b illustrations, digital file 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
490 1 |a Biomedical and nanomedical technologies 
500 |a Title from PDF title page (viewed on September 27, 2012). 
504 |a Includes bibliographical references (pages 59-69). 
505 0 |a Introduction. 
505 8 |a 1. Drug delivery nanosystems as a promising area of modern chemistry and medicine. Silica nanoparticles as potential drug carriers. 
505 8 |a 2. Syntheses of mesoporous silica materials -- 2.1 Syntheses of unmodified silica materials -- 2.2 Synthesis of modified silica materials. 
505 8 |a 3. Characterization of silica materials as potential carriers for GMDP. -- 3.1 Characterization of silica materials via FTIR spectroscopy -- 3.2 Characterization of silica materials via nitrogen adsorption-desorption measurements -- 3.3 Particle size of silica materials -- 3.4 Characterization of silica materials via small angle x-ray scattering (SAXS) -- 3.5 Adsorption properties of silica materials -- 3.6 DSC study of composites of model protein with silica materials -- 3.7 Calorimetric study of adsorption of model protein on silica materials -- 3.8 Preparation of silica nanoparticle suspensions. 
505 8 |a 4. Interaction of silica nanoparticles with immune system cells -- 4.1 Intensity of different silica nanoparticles uptake by immune cells -- 4.2 Influence of silica nanoparticles on parameters of functional activity of peritoneal macrophages. 
505 8 |a 5. Peritoneal macrophages of women with endometriosis as a possible target for immunomodulatory drugs -- 5.1 Impairment of peritoneal macrophage function at endometriosis -- 5.2 Influence of glucosaminyl muramyldipeptide upon functional activity of peritoneal macrophages of women with endometriosis. 
505 8 |a 6. Effectiveness of different types of silica nanoparticles as drug carriers for topical delivery of GMDP into peritoneal macrophages of women with endometriosis -- 6.1 Immobilization of GMDP on silica nanoparticles -- 6.2 Comparative study of the effects of free GMDP and GMD immobilized on silica nanoparticles on the functional state of peritoneal macrophages. 
505 8 |a References. 
520 3 |a The development of nanosystems for topical drug delivery to target cells is a promising tool to improve the drug therapeutic index. Transport systems can be designed to control the dispatch of the loaded drug to target areas, increasing its local concentration and bioavailability, while prolonging its retention, half-life and effectiveness. Therefore, such "smart" nanodevices are able to change radically the practice of therapy for a variety of diseases and disorders. The purpose of this book is to present the recent research development of nanoparticulate delivery systems for immune modulating agent, glucosaminyl muramyldipeptides (N-acetylglucosaminyl-Nacetylmuramyl- L-alanyl-D-isoglutamine) or GMDP, which is the main component of bacterial wall with known target of action through NOD2 receptors, with an overlook to their applications for treatment of endometriosis, which often results in infertility. Silica-based nanoparticles have generated a significant amount of interest because of their inherent properties. 
590 |a eBooks on EBSCOhost  |b EBSCO eBook Subscription Academic Collection - Worldwide 
650 0 |a Drug delivery systems. 
650 0 |a Nanosilicon. 
650 0 |a Immunological adjuvants. 
650 0 |a Nanomedicine. 
650 0 |a Nanoparticles. 
650 0 |a Endometriosis  |x Treatment. 
650 0 |a Nanotechnology. 
650 0 |a Silicon. 
650 2 |a Adjuvants, Immunologic 
650 2 |a Drug Delivery Systems 
650 2 |a Endometriosis  |x therapy 
650 2 |a Nanomedicine 
650 2 |a Nanoparticles 
650 2 |a Silicon 
650 6 |a Systèmes d'administration de médicaments. 
650 6 |a Nanosilicium. 
650 6 |a Adjuvants immunologiques. 
650 6 |a Nanoparticules. 
650 6 |a Endométriose  |x Traitement. 
650 6 |a Nanomédecine. 
650 6 |a Silicium. 
650 7 |a silicon.  |2 aat 
650 7 |a MEDICAL  |x Pharmacology.  |2 bisacsh 
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650 7 |a Nanotechnology.  |2 fast  |0 (OCoLC)fst01032639 
650 7 |a Drug delivery systems.  |2 fast  |0 (OCoLC)fst00898667 
650 7 |a Endometriosis  |x Treatment.  |2 fast  |0 (OCoLC)fst00909776 
650 7 |a Immunological adjuvants.  |2 fast  |0 (OCoLC)fst00967992 
650 7 |a Nanomedicine.  |2 fast  |0 (OCoLC)fst01744350 
650 7 |a Nanoparticles.  |2 fast  |0 (OCoLC)fst01032624 
650 7 |a Nanosilicon.  |2 fast  |0 (OCoLC)fst01744914 
653 |a Mesoporous silica 
653 |a nanoparticles 
653 |a sol-gel synthesis 
653 |a surface functionalization 
653 |a glucosaminyl muramyldipeptide 
653 |a endometriosis 
653 |a drug delivery system 
653 |a drug immobilization 
653 |a blood lymphocytes 
653 |a peritoneal macrophages 
653 |a scavenger receptors 
653 |a functional activity of the immune cells 
700 1 |a Parfenyuk, E. V. 
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